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2. Interactions between heterologous forms of prion protein: binding, inhibition of conversion, and species barriers. Horiuchi M; Priola SA; Chabry J; Caughey B Proc Natl Acad Sci U S A; 2000 May; 97(11):5836-41. PubMed ID: 10811921 [TBL] [Abstract][Full Text] [Related]
3. Specific binding of normal prion protein to the scrapie form via a localized domain initiates its conversion to the protease-resistant state. Horiuchi M; Caughey B EMBO J; 1999 Jun; 18(12):3193-203. PubMed ID: 10369660 [TBL] [Abstract][Full Text] [Related]
4. Sulfated glycans and elevated temperature stimulate PrP(Sc)-dependent cell-free formation of protease-resistant prion protein. Wong C; Xiong LW; Horiuchi M; Raymond L; Wehrly K; Chesebro B; Caughey B EMBO J; 2001 Feb; 20(3):377-86. PubMed ID: 11157745 [TBL] [Abstract][Full Text] [Related]
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9. Efficient conversion of normal prion protein (PrP) by abnormal hamster PrP is determined by homology at amino acid residue 155. Priola SA; Chabry J; Chan K J Virol; 2001 May; 75(10):4673-80. PubMed ID: 11312338 [TBL] [Abstract][Full Text] [Related]
10. A single hamster PrP amino acid blocks conversion to protease-resistant PrP in scrapie-infected mouse neuroblastoma cells. Priola SA; Chesebro B J Virol; 1995 Dec; 69(12):7754-8. PubMed ID: 7494285 [TBL] [Abstract][Full Text] [Related]
11. Formation of protease-resistant prion protein in cell-free systems. Caughey B Curr Issues Mol Biol; 2000 Jul; 2(3):95-101. PubMed ID: 11471561 [TBL] [Abstract][Full Text] [Related]
12. In situ formation of protease-resistant prion protein in transmissible spongiform encephalopathy-infected brain slices. Bessen RA; Raymond GJ; Caughey B J Biol Chem; 1997 Jun; 272(24):15227-31. PubMed ID: 9182546 [TBL] [Abstract][Full Text] [Related]
13. Molecular assessment of the potential transmissibilities of BSE and scrapie to humans. Raymond GJ; Hope J; Kocisko DA; Priola SA; Raymond LD; Bossers A; Ironside J; Will RG; Chen SG; Petersen RB; Gambetti P; Rubenstein R; Smits MA; Lansbury PT; Caughey B Nature; 1997 Jul; 388(6639):285-8. PubMed ID: 9230438 [TBL] [Abstract][Full Text] [Related]
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16. The glycosylation status of PrPC is a key factor in determining transmissible spongiform encephalopathy transmission between species. Wiseman FK; Cancellotti E; Piccardo P; Iremonger K; Boyle A; Brown D; Ironside JW; Manson JC; Diack AB J Virol; 2015 May; 89(9):4738-47. PubMed ID: 25673720 [TBL] [Abstract][Full Text] [Related]
17. Pathogenic mutations within the hydrophobic domain of the prion protein lead to the formation of protease-sensitive prion species with increased lethality. Coleman BM; Harrison CF; Guo B; Masters CL; Barnham KJ; Lawson VA; Hill AF J Virol; 2014 Mar; 88(5):2690-703. PubMed ID: 24352465 [TBL] [Abstract][Full Text] [Related]
18. Chaperone-supervised conversion of prion protein to its protease-resistant form. DebBurman SK; Raymond GJ; Caughey B; Lindquist S Proc Natl Acad Sci U S A; 1997 Dec; 94(25):13938-43. PubMed ID: 9391131 [TBL] [Abstract][Full Text] [Related]